Product Code Database
Example Keywords: grand theft -netbooks $32
   » » Wiki: Holmium
Tag Wiki 'Holmium'.
Tag

Holmium is a ; it has symbol Ho and 67. It is a rare-earth element and the eleventh member of the lanthanide series. It is a relatively soft, silvery, fairly -resistant and metal. Like many other lanthanides, holmium is too reactive to be found in native form, as pure holmium slowly forms a yellowish coating when exposed to air. When isolated, holmium is relatively stable in dry air at room temperature. However, it reacts with water and corrodes readily, and also burns in air when heated.

In nature, holmium occurs together with the other rare-earth metals (like ). It is a relatively rare lanthanide, making up 1.4 parts per million of the Earth's crust, an abundance similar to . Holmium was discovered through isolation by Swedish chemist Per Theodor Cleve. It was also independently discovered by Jacques-Louis Soret and Marc Delafontaine, who together observed it in 1878. Its oxide was first isolated from rare-earth ores by Cleve in 1878. The element's name comes from Holmia, the Latin name for the city of .

Like many other , holmium is found in the minerals and and is usually commercially extracted from monazite using techniques. Its compounds in nature and in nearly all of its laboratory chemistry are trivalently oxidized, containing Ho(III) . Trivalent holmium ions have properties similar to many other rare-earth ions (while yielding their own set of unique emission light lines), and thus are used in the same way as some other rare earths in certain and glass-colorant applications.

Holmium has the highest magnetic permeability and magnetic saturation of any element and is thus used for the of the strongest static . Because holmium strongly absorbs , it is also used as a in .


Properties
Holmium is the eleventh member of the series. In the periodic table, it appears in period 6, between the lanthanides to its left and to its right, and above the .


Physical properties
With a boiling point of , holmium is the sixth most volatile lanthanide after , , , and . At standard temperature and pressure, holmium, like many of the second half of the lanthanides, normally assumes a hexagonally close-packed (hcp) structure. Its 67 are arranged in the configuration Xe 4f11 6s2, so that it has thirteen filling the 4f and 6s subshells.

Holmium, like all of the lanthanides, is at standard temperature and pressure. However, holmium is at temperatures below . It has the highest () of any naturally occurring element and possesses other unusual magnetic properties. When combined with , it forms highly compounds.


Chemical properties
Holmium metal tarnishes slowly in air, forming a yellowish oxide layer that has an appearance similar to that of rust. It burns readily to form holmium(III) oxide:

4 Ho + 3 O2 → 2 Ho2O3

It is a relatively soft and element that is fairly -resistant and chemically stable in dry air at standard temperature and pressure. In moist air and at higher temperatures, however, it quickly , forming a yellowish oxide. In pure form, holmium possesses a metallic, bright silvery luster.

Holmium is quite electropositive: on the Pauling electronegativity scale, it has an electronegativity of 1.23. It is generally trivalent. It reacts slowly with cold water and quickly with hot water to form holmium(III) hydroxide:

2 Ho (s) + 6 H2O (l) → 2 Ho(OH)3 (aq) + 3 H2 (g)

Holmium metal reacts with all the stable :

2 Ho (s) + 3 F2 (g) → 2 HoF3 (s) pink

2 Ho (s) + 3 Cl2 (g) → 2 HoCl3 (s) yellow

2 Ho (s) + 3 Br2 (g) → 2 HoBr3 (s) yellow

2 Ho (s) + 3 I2 (g) → 2 HoI3 (s) yellow

Holmium dissolves readily in dilute to form solutions containing the yellow Ho(III) ions, which exist as a Ho(OH2)93+ complexes:

2 Ho (s) + 3 H2SO4 (aq) → 2 Ho3+ (aq) + 3 (aq) + 3 H2 (g)


Oxidation states
As with many lanthanides, holmium is usually found in the +3 , forming compounds such as holmium(III) fluoride (HoF3) and holmium(III) chloride (HoCl3). Holmium in solution is in the form of Ho3+ surrounded by nine molecules of water. Holmium dissolves in . However, holmium is also found to exist in +2, +1 and 0 oxidation states.


Isotopes
Natural holmium consists of one primordial isotope, holmium-165. It is observationally stable, though theoretically should undergo to terbium-161 with a very long half-life.

The known isotopes of holmium range from 140Ho to 175Ho. The primary before the 165Ho, is beta plus decay to dysprosium isotopes, and the primary mode after is beta minus decay to . Of the 35 synthetic radioactive isotopes among these, the most stable one is holmium-163 (163Ho), with a half-life of 4570 years. The next most stable is holmium-166 (166Ho) having a half-life of 26.812 hours, and others have half-lives under 4 hours.

The 166m1Ho has the unusually long half-life of 1133 years. With a very low excitation energy, it does not decay to the ground state but beta-decays directly, having a particularly rich spectrum of , making this isotope useful as a means for gamma ray spectrometers.

Holmium-166 (ground state) has been studied for medical application.


Compounds

Oxides and chalcogenides
Holmium(III) oxide is the only oxide of holmium. It changes its color depending on the lighting conditions. In daylight, it has a yellowish color. Under , it appears orange red, almost indistinguishable from the appearance of erbium oxide under the same lighting conditions. The color change is related to the sharp of trivalent holmium ions acting as red phosphors. Holmium(III) oxide appears pink under a cold-cathode fluorescent lamp.

Other are known for holmium. Holmium(III) sulfide has orange-yellow in the monoclinic crystal system, with the P21/ m (No. 11).

(2025). 9783540649663, Springer.
Under high pressure, holmium(III) sulfide can form in the cubic and orthorhombic . It can be obtained by the reaction of holmium(III) oxide and at . Holmium(III) selenide is also known. It is antiferromagnetic below 6 K.


Halides
All four trihalides of holmium are known. Holmium(III) fluoride is a yellowish powder that can be produced by reacting holmium(III) oxide and ammonium fluoride, then crystallising it from the ammonium salt formed in solution. Holmium(III) chloride can be prepared in a similar way, with ammonium chloride instead of ammonium fluoride. It has the YCl3 layer structure in the solid state. These compounds, as well as holmium(III) bromide and holmium(III) iodide, can be obtained by the direct reaction of the elements:

2 Ho + 3 X2 → 2 HoX3

In addition, holmium(III) iodide can be obtained by the direct reaction of holmium and mercury(II) iodide, then removing the mercury by .


Organoholmium compounds
Organoholmium compounds are very similar to those of the other lanthanides, as they all share an inability to undergo . They are thus mostly restricted to the mostly ionic cyclopentadienides ( with those of lanthanum) and the σ-bonded simple and , some of which may be .Greenwood and Earnshaw, pp. 12481249


History
Holmium (Holmia, name for ) was discovered by the Swiss chemists Jacques-Louis Soret and Marc Delafontaine in 1878 who noticed the aberrant spectrographic emission spectrum of the then-unknown element (they called it "Element X").

The Swedish chemist Per Teodor Cleve also independently discovered the element while he was working on earth (). He was the first to isolate impure oxide of the new element. Using the method developed by the Swedish chemist Carl Gustaf Mosander, Cleve first removed all of the known contaminants from erbia. The result of that effort was two new materials, one brown and one green. He named the brown substance holmia (after the Latin name for Cleve's home town, Stockholm) and the green one thulia. Holmia was later found to be the , and thulia was . The pure oxide was only isolated in 1911 and the metal in 1939 by Heinrich Bommer.

(2025). 9783662689202, Springer Berlin Heidelberg. .

In the English physicist 's classic paper on , holmium was assigned the value 66. The holmium preparation he had been given to investigate had been impure, dominated by neighboring dysprosium. He would have seen x-ray emission lines for both elements, but assumed that the dominant ones belonged to holmium, instead of the dysprosium impurity.


Occurrence and production
Like all the other rare-earth elements, holmium is not naturally found as a . It occurs combined with other elements in gadolinite, and other rare-earth minerals. No holmium-dominant mineral has yet been found. The main mining areas are China, United States, Brazil, India, Sri Lanka, and Australia with reserves of holmium estimated as 400,000 tonnes. The annual production of holmium metal is of about 10 tonnes per year.

Holmium makes up 1.3 parts per million of the Earth's crust by mass.ABUNDANCE OF ELEMENTS IN THE EARTH'S CRUST AND IN THE SEA, CRC Handbook of Chemistry and Physics, 97th edition (2016–2017), p. 14-17 Holmium makes up 1 part per million of the , 400 parts per quadrillion of seawater, and almost none of Earth's atmosphere, which is very rare for a lanthanide. It makes up 500 parts per trillion of the universe by mass.

Holmium is commercially extracted by from monazite sand (0.05% holmium), but is still difficult to separate from other rare earths. The element has been isolated through the of its or with metallic . Its estimated abundance in the Earth's crust is 1.3 mg/kg. Holmium obeys the Oddo–Harkins rule: as an odd-numbered element, it is less abundant than both dysprosium and erbium. However, it is the most abundant of the odd-numbered heavy . Of the lanthanides, only , , lutetium and terbium are less abundant on Earth. The principal current source are some of the ion-adsorption clays of southern China. Some of these have a rare-earth composition similar to that found in or gadolinite. Yttrium makes up about two-thirds of the total by mass; holmium is around 1.5%.

(2025). 9780070494398, McGraw-Hill. .
Holmium is relatively inexpensive for a rare-earth metal with the price about 1000 /kg.


Applications
Glass containing holmium oxide and holmium oxide solutions (usually in ) have sharp optical absorption peaks in the spectral range 200 to 900 nm. They are therefore used as a calibration standard for . The radioactive but long-lived 166m1Ho is used in calibration of gamma-ray spectrometers.

Holmium is used to create the strongest artificially generated , when placed within high-strength magnets as a magnetic pole piece (also called a magnetic flux concentrator). Holmium is also used in the manufacture of some .

Holmium can act as a sensitizer in sodium yttrium fluoride which takes advantage of its absorption in the NIR-II window. Holmium allows for lanthanide nanomaterials to have tunable emission and excitation in the NIR-II. Under 1143 nm excitation the interfacial energy transfer to other lanthanides allows a redshift in emission for biological applications. This allows deeper penetration than typically used 980 nm and 808 nm lasers.

Holmium-doped yttrium iron garnet (YIG) and yttrium lithium fluoride have applications in solid-state lasers, and Ho-YIG has applications in and in equipment (e.g., ). Holmium lasers emit at 2.1 micrometres. They are used in medical, dental, and applications.

(2025). 9780415333405, CRC Press. .
It is also used in the enucleation of the .

Since holmium can absorb -bred neutrons, it is used as a to regulate nuclear reactors. It is used as a for , providing pink coloring, and for , providing yellow-orange coloring. In March 2017, announced that they had developed a technique to store one of data on a single holmium atom set on a bed of . With sufficient quantum and classical control techniques, holmium may be a good candidate to make quantum computers.

Holmium is used in the medical field, particularly in for procedures such as kidney stone removal and prostate treatment, due to its precision and minimal tissue damage. Its , holmium-166, is applied in targeted cancer therapies, especially for liver cancer, and it also enhances imaging as a contrast agent.


Biological role and precautions
Holmium plays no biological role in humans, but its salts are able to stimulate .
(2025). 9780849304811, CRC press.
Humans typically consume about a milligram of holmium a year. Plants do not readily take up holmium from the soil. Some vegetables have had their holmium content measured, and it amounted to 100 parts per trillion. Holmium and its soluble salts are slightly toxic if ingested, but insoluble holmium salts are . Metallic holmium in dust form presents a fire and explosion hazard. Large amounts of holmium salts can cause severe damage if , consumed , or injected. The biological effects of holmium over a long period of time are not known. Holmium has a low level of .


See also


Bibliography


Further reading
  • R. J. Callow, The Industrial Chemistry of the Lanthanons, Yttrium, Thorium, and Uranium, Pergamon Press, 1967.


External links
  • Holmium at The Periodic Table of Videos (University of Nottingham)

Page 1 of 1
1
Page 1 of 1
1

Account

Social:
Pages:  ..   .. 
Items:  .. 

Navigation

General: Atom Feed Atom Feed  .. 
Help:  ..   .. 
Category:  ..   .. 
Media:  ..   .. 
Posts:  ..   ..   .. 

Statistics

Page:  .. 
Summary:  .. 
1 Tags
10/10 Page Rank
5 Page Refs
1s Time